Clinical Research Software

Our Clinical Research Software is designed to streamline research, study management and data analysis while being super flexible for your specific research needs. Experience efficiency and accuracy like never before in your research endeavors.

government case management software

A Master Clinical Research System.

Streamline workflows, administrative tasks, and medical trial management with our all-in-one solution.

Highlights of Clinical Research Software

Beyond just managing clinical research and trials, our software is a catalyst for innovation in research. It enables researchers to get deeper insights from data, facilitates seamless collaboration across different teams and institutions, and accelerate the pace of medical discoveries. The software's adaptability to various research methodologies makes it a versatile tool for a wide range of clinical studies, from small-scale investigations to large, multi-center trials.

Trial Management
Data Analysis
Regulatory Compliance
Patient Enrollment

Clinical Research Software Modules

Clinical Research Software

Key Features of Clinical Research Software

  1. Streamlines the entire lifecycle of clinical research and trials for efficient management.
  2. Offers powerful statistical tools for thorough and accurate data analysis.
  3. Ensures adherence to global regulatory standards and ethical guidelines.
  4. Simplifies patient recruitment and consent processes with intuitive interfaces.
  5. Facilitates collaboration among researchers, institutions, and stakeholders.
  6. Implements stringent security protocols to protect sensitive clinical data.

Clinical Research Software Capabilities

Comprehensive Trial Dashboard
Automated Data Collection
Real-Time Data Monitoring
Advanced Statistical Analysis
Secure Data Storage and Access
Integration with Medical Records
servicerocket a versatile itsm automation tool's dashboard
sysaid itsm automation tool's dashboard for streamlining it services

Related Healthcare Software

What is Next?

  • Get help building your app: Request a demo and we'll install this application to your trial Kohezion account. 

Frequently Asked Questions

Kohezion's Clinical Research Software is an innovative solution for researchers and healthcare professionals. It offers an integrated platform for managing clinical research, from patient enrollment to data collection and analysis. The software provides robust tools for statistical analysis, ensuring high-quality, reliable results. With its advanced HIPAA-compliant data security measures, it is ideal for simplifying complex research processes, enhancing collaboration among researchers, and ensuring compliance with regulatory standards.

  1. Study Design and Setup
    • Design and set up clinical research, trials, including protocols and methodologies, in the 'Study Design' module. Ensure alignment with research objectives and compliance standards.
  2. Participant Management
    • Manage participant recruitment, enrollment, and tracking in the 'Participant Management' section. Maintain participant data securely and manage consent forms.
  3. Data Collection and Management
    • Collect, store, and manage clinical trial data in the 'Data Management' module. Use electronic data capture (EDC) systems for efficient and accurate data collection.
  4. Regulatory Compliance and Submission
    • Ensure compliance with regulatory requirements and manage submissions to regulatory bodies in the 'Regulatory Compliance' section. Keep track of submission deadlines and requirements.
  5. Study Monitoring and Site Management
    • Oversee clinical study progress and manage site activities in the 'Study Monitoring' module. Conduct site visits and audits to ensure study integrity.
  6. Adverse Event and Safety Reporting
    • Track and report adverse events and safety incidents in the 'Safety Reporting' section. Ensure timely reporting in compliance with regulatory guidelines.
  7. Data Analysis and Statistical Reporting
    • Analyze clinical trial data and generate statistical reports in the 'Data Analysis' module. Utilize advanced statistical tools for comprehensive data interpretation.
  8. Document Management and eTMF
    • Manage study-related documents and maintain an electronic Trial Master File (eTMF) in the 'Document Management' section. Ensure easy access and organization of critical documents.
  9. Financial Management and Budgeting
    • Handle financial aspects of clinical trials, including budgeting and invoicing, in the 'Financial Management' module. Track study costs and manage funding.
  10. Collaboration and Communication Tools
    • Facilitate collaboration among research teams, sponsors, and stakeholders using integrated communication tools in the 'Collaboration' section.
marine mammal
university of san francisco
iniversity of illinois
Scroll to Top